Primary Orbital Respiratory Epithelial Cyst: A Systematic Review and Two Case Reports

Author:

Laezza Maria Paola1,Alqahtani Reham2,Lanni Vittoria3,Iuliano Adriana3,Althaqib Rawan N.2,Maktabi Azza4,Costagliola Ciro3,Strianese Diego3

Affiliation:

1. Department of Medicine and Health Sciences, University of Molise, Campobasso, Italy

2. Oculoplastic Division, King Khalid Eye Specialist Hospital, Riyadh, Saudi Arabia

3. Department of Neurosciences, Reproductive Sciences, and Dentistry, University of Naples Federico II, Naples, Italy

4. Pathology Department, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia

Abstract

A primary orbital respiratory cyst is a congenital choristoma that presents in the orbit and with different signs and symptoms depending on the location, which might also change the surgical approach. The aim of this report is to describe 2 new cases of primary respiratory epithelial cysts and to review the literature on presentation, management, and risk factors with different surgical approaches and complications. Two cases presenting with gradually increased proptosis had a confirmed diagnosis of a respiratory epithelial cyst. CT and MRI imaging revealed a thin-walled intraconal cystic lesion. Complete surgical removal was not possible and an incisional biopsy of the wall was performed. Rarely, orbital respiratory epithelium cysts are primary lesions. The high risk of breaking the capsule during surgery and the presence of residual epithelial cells within the orbit may cause cyst’s recurrence. Indeed, we recommend careful attention during dissection maneuvers and a long-term follow-up.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference17 articles.

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